Portable universal inhaler system

ABSTRACT

A portable universal inhaler system formed from an outer part and an inner part slidably received in the outer part. The inner part defines a compartment for receiving a medication canister and includes a universal connector for making a fluid dispensing connection to a variety of commercially available canisters. The inner and outer parts, when assembled, together form a housing that defines a chamber of sufficient volume to house a metered dose of medication. A mouthpiece or mouthpiece attachment location is provided in fluid communication with the chamber for permitting inhalation of medication from the chamber. The structure of the device makes it compact and portable, in the closed position, allows for storage of a medication canister in operative engagement with the device, and provides a convenient way to dispense medication, using a medication canister and a chamber, for inhalation by a user.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation U.S. patent application Ser. No.11/223,625, filed on Sep. 9, 2005, currently pending, the disclosure ofwhich is hereby incorporated by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to a portable universal inhaler system foreffectively delivering medications by inhalation through the mouth. Morespecifically, the present invention relates to a portable inhaler systemthat can be used with a variety of different medication canisters.

BACKGROUND OF THE INVENTION

The delivery of a metered dose of medication via inhalation into thelungs is a common method used for administration of a variety of drugs,including, but not limited to, asthma medications, insulin, steroids andtreatments for pulmonary diseases. Although the metered dose inhalercanister dispenses a fixed, metered dose of medication, only a portionof the metered dose actually reaches the lungs of a patient. Even ifinhalation is properly timed with the dispensing of the medication fromthe inhaler, the amount of medication reaching the lungs isinconsistent, depending on various factors including the quantity ofmedication dissolved and/or entrained in the air entering the patient'slungs, and the quantity of medication that is deposited on one or moresurfaces of the inhaler, the mouth and/or oropharyngeal area of thepatient. Deposition of medication in the mouth or oropharyngeal area ofthe patient can cause complications, such as candidiasis, and may leavean unpleasant aftertaste.

Many patients also have practical problems with the use of inhalers,such as difficulty compressing the dose canister, difficulty in timinginhalation with the dispensing of medication, and an inability to inhalea full dose of medication in a single breath. In practice, patientsfrequently activate an inhaler multiple times in order to dispense asingle dose, despite the fact that the desired metered dose should havebeen dispensed via a single activation of the inhaler. This is adocumented response to the difficulty and inconsistency of medicationdelivery, which response undermines the effectiveness of metered doseinhalers, thereby leading to concerns such as over-medication,under-medication, and waste, as well as higher costs for treatment. Theproblem with improper storage and difficulty with sterilizationtechniques also poses risk for further unwanted fungal and bacterialinfections.

One proposed solution to the problem of inconsistent dosing has been toprovide a “spacer” or “chamber” within the inhalation device, typicallyin the form of a reservoir of air. The spacer or chamber provides alocation for mixing the metered dose of medication with air beforeinhalation, thereby potentially reducing the inconsistency of dosing dueto timing difficulties. U.S. Pat. Nos. 4,470,412; 4,790,305; 4,926,852;5,012,803; 5,040,527; 5,042,467; 5,816,240; and 6,026,807 disclosevarious devices of this type.

Additionally, some devices with spacers have been provided with a valvemechanism to permit inhalation of a single dose of medication in morethan one breath. For example, see U.S. Pat Nos. 4,470,412 and 5,385,140.The articles, Demirkan, et al., “Salmeterol Administration byMetered-Dose Inhaler Alone vs. Metered-Dose Inhaler Plus Valved HoldingChamber,” Chest, 117 (2000) pp. 1314-1318, Finlay and Zuberbuhler, “Invitro comparison of beclomethasone and salbutamol metered-dose inhaleraerosols inhaled during pediatric tidal breathing from four valvedholding chambers,” Chest, 114 (1998) pp. 1676-1680, and Konig, “Spacerdevices used with metered-dose inhalers. Breakthrough or gimmick?”Chest, 88 (1985) pp. 276-284; also provide information in relation tosuch devices.

For infants or other patients who have difficulty using a mouthpiece, amask is commonly attached or incorporated onto the inhaler. See U.S.Pat. Nos. 4,809,692; 4,832,015; 5,012,804; 5,427,089; 5,645,049 and5,988,160. Also, some devices include an audible signaling device towarn patients when inhalation exceeds a desirable rate, e.g. U.S. Pat.Nos. 4,809,692 and 5,042,467.

One method of attaching a spacer to a canister of a metered dose inhaleris to insert the inhaler into a universal adapter such as that shown inU.S. Pat. No. 5,848,588, but this is bulky and awkward to use. Otherdevices are designed to have a specific canister inserted into thedevice. It would be beneficial to be able to insert different canistersinto a single inhaler.

Accordingly, in view of the foregoing, there remains a need for aneasily portable, universal inhaler system that can be easily used andcleaned. There is also a need for a design that permits the use ofattachments for infants, if desired. These and other objects of variousembodiments of the invention are addressed by one or more of theembodiments of the invention described below. It should be understood,however, that specific embodiments of the invention need not addresseach and every object listed herein in order to be considered part ofthe inventive concept.

SUMMARY OF THE INVENTION

In one aspect, the present invention relates to an inhaler system thatincludes structure that permits insertion of different medicationcanisters.

In another aspect, the present invention relates to an inhaler systemthat is easily portable and includes structure that permits insertion ofdifferent medication canisters. In this aspect, the inhaler systemincludes at least two parts, one of which parts fits at least partiallywithin another part to thereby enhance the portability of the device.

In another aspect, the present invention relates to an inhaler systemthat can be easily cleaned and/or sterilized. In this aspect, theinhaler system includes two or more parts that can be readilydisassembled and reassembled to allow thorough cleaning or sterilizationof the surfaces of the device.

BRIEF DESCRIPTION OF THE DRAWINGS

For the purpose of illustrating the invention, representativeembodiments are shown in the accompanying figures, it being understoodthat the invention is not intended to be limited to the precisearrangements and instrumentalities shown.

FIG. 1 is a top view of one embodiment of an inhaler system of thepresent invention, in the closed position.

FIG. 2 is a side view of the inhaler system of FIG. 1 in the closedposition.

FIG. 3 is an end view of the inhaler system of FIG. 1 in the closedposition.

FIGS. 4-6 are top, side and end views, respectively, of the cover of theinhaler system of FIGS. 1-3.

FIG. 7 is a top view of the inner part of the inhaler system shown inFIGS. 1-3.

FIG. 8 is a cross-sectional view of a portion of the inner part of theinhaler system of FIGS. 1-3.

FIG. 9 is a detail view of the portion IX of FIG. 8.

FIG. 10 is a sagittal plane cross-sectional view of one embodiment ofthe outer part of FIGS. 1-3.

FIG. 11 is a horizontal plane cross-sectional view of the outer part ofFIG. 10.

FIG. 12 is an end view of the outer part of FIG. 10.

FIGS. 13A-13B are cross-sectional views of nozzle outlets includingfluid mixing structure.

FIG. 14 is a side view of the inhaler system of FIGS. 1-3 in the openposition.

FIG. 15 is a bottom view of the inhaler system of FIGS. 1-3 in the openposition.

FIG. 16 is an end view of the inhaler system of FIGS. 1-3 in the openposition.

FIG. 17 is a cross-sectional view of an alternative embodiment of theinner part of the inhaler system.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to FIGS. 1-3, there is shown an embodiment of an inhalersystem 10 in accordance with the present invention, depicted in theclosed position. The closed position of inhaler system 10 is designedfor storage and transport of the inhaler system 10. In the closedposition of FIGS. 1-3, the inhaler system is relatively small and canfit, for example, into a clothing pocket for storage or transport.Moreover, in this closed position, the inhaler system 10 houses at leastone medication canister therein, thereby eliminating the need to carry amedication canister separately from system 10.

In FIG. 1, is shown a top view of inhaler system 10 in the closedposition. Inhaler system 10 includes an outer part 12 and an inner part14, which together form a housing. Inner part 14 is sized to fit withinouter part 12, optionally with a friction-fit, form fit or another typeof fit that creates a seal between inner part 14 and outer part 12 toprovide a substantially airtight chamber 18 within outer and inner parts12, 14, when they are fitted together in at least the open position.

Inner part 14 includes a canister compartment 20 into which a canistercan be inserted. Canister compartment 20 is adapted to be substantiallyuniversal in that it is designed to accept canisters of different sizesand lengths. Tapered opening 22 of compartment 20 facilitates insertionand removal of different sized canisters into compartment 20 of innerpart 14, by providing an area from which the canister can protrudeoutwardly from compartment 20. Since tapered opening 22 is tapered, asshown, compartment 20 can accommodate canisters of different lengths,while still permitting the user to depress the canister withincompartment 20 in order to dispense a metered dose of medication fromthe canister. Compartment 20 is sized to have a diameter whichaccommodates one of the widest, if not the widest, of the commerciallyavailable canisters so that canisters of smaller diameters can also befit into compartment 20 of inner part 14.

FIG. 2 depicts a side view of the inhaler system 10 of FIG. 1 in aclosed position. In FIG. 2, cover 16 of inhaler system 10 is shown.Cover 16 provides a convenient way to close inhaler system 10 and mayalso be employed to retain outer and inner parts 12, 14 together in boththe open and closed positions. The inner surface 24 of cover 16 is aconvenient location to provide product information, product literature,and/or instructions for use of inhaler system 10. Cover 16 may also beprovided with a grasping structure 19 for facilitating grasping of cover16 by the user to open and close cover 16. Any suitable, conventionalgrasping structure may be employed.

FIG. 3 shows an end view of inhaler system 10 of FIG. 1 in a closedposition. From this view, it can be seen that cover 16 includes a tab 17that extends down and over a portion of the end of inhaler system 10.The purpose of tab 17 is to cover mouthpiece 40 of inner part 14.Referring to FIGS. 4-6, three different views of cover 16 are shown,with these views corresponding to the views of the inhaler system 10seen in FIGS. 1-3. In FIGS. 4 and 6, it can be seen that cover 16 mayinclude a two pegs 26 which are designed to fit into correspondingrecesses 28 in outer part 12. In this manner, cover 16 can be releasablysecured to outer part 12 by locating pegs 26 in recesses 28. Also, thismanner of mounting cover 16 to outer part 12 permits cover 16 to pivotabout pegs 26 to permit opening and closing of the cover 16, as shown,without removing the cover 16 from the outer part 12. Any othersuitable, conventional structure for mounting cover 16 onto outer part12 may be employed, so long as cover 16 can be easily removed from outerpart 12 to permit cleaning of the inhaler system 10, and cover 16 canpivot about an axis located approximately between the locations of pegs26 of cover 16, relative to outer part 12, to allow opening and closingof cover 16.

Referring to FIGS. 7-9, there are shown three views of inner part 14 ofinhaler system 10. Inner part 14 may be designed to be slidably receivedwithin outer part 12 and thus is slightly smaller than outer part 12 sothat inner part 14 fits within outer part 12. Inner part 14 forms acompartment 20 for receiving a canister which may contain medication.Inner part 14 also includes a handle 30 which can be formed by, forexample, texturing a portion of the surface of inner part 14, as shownin FIG. 7. Other forms of suitable handles 30 may be employed, such asan indentation in part of the surface, an attached structure suitablefor grasping, etc. Handle 30 is employed by the user to move inner part14 from the closed position of FIGS. 1-3 wherein most of inner part 14is located within outer part 12, to the open position of FIGS. 10-12,wherein at least a substantial portion of inner part 14 protrudes fromouter part 12 sufficiently to allow insertion of a canister intocompartment 20 of inner part 14 via tapered opening 22.

Also part of inner part 14 is nozzle assembly 32. Nozzle assembly 32includes a nozzle inlet 34 and a nozzle outlet 36. Nozzle inlet 34 isdesigned for fluid connection to a canister to dispense medication fromthe canister. Nozzle outlet 36 is in fluid communication with nozzleinlet 34 and directs fluid from nozzle inlet 34 into chamber 18 ofinhaler system 10. Any conventional, suitable nozzle assembly 32 may beemployed. Optionally, nozzle inlet 34 includes a conventional universalconnector, not shown, that it is adapted to attach to a variety ofdifferent canisters.

In operation, a canister is operatively connected to nozzle inlet 34, ina conventional manner. A portion of the canister will protrude fromcompartment 20 through tapered opening 22. The user will depress theprotruding portion of the canister to dispense a metered dose ofmedication from the canister to the nozzle inlet 34. The metered dose ofmedication then proceeds to chamber 18 via nozzle outlet 36.

In an optional embodiment, nozzle outlet 36 includes structure formixing the medication with air as it flows through nozzle outlet 36.Such structure may include, for example, a series of baffles, or aswirler shaped, for example, like a screw. The medication is forcedthrough the mixing structure to chamber 18 to provide intimate mixing ofair and medication to thereby entrain or disperse a greater amount ofmedication in air in chamber 18, than would be entrained or dispersedwithout a mixing structure. One suitable structure of nozzle outlet 36,including a series of baffles 38, is shown, for example, in FIG. 13A. Asuitable swirler 42 included in nozzle outlet 36 is depicted in FIG.13B. In one embodiment, the swirler 42 may be mounted for rotationalmovement about an axis to enhance mixing of the medication with air.Alternatively, baffles 38 or swirler 42 can be located in nozzle inlet34, nozzle outlet 36, as shown, both locations, or combinations ofbaffles 38 and one or more swirlers 42 may also be employed. Onesuitable swirler 42 is available from Amici.

In another optional embodiment, inhaler system 10 may be provided with acounter 44, shown schematically in FIG. 11. Counter 44 may include abutton 46 and an indicator 48 to allow the user to keep track of thenumber of doses dispensed from a particular canister. Since mostconventional canisters are designed to dispense a predetermined numberof metered doses, and are not provided with a means to indicate how muchmedication remains in the canister, keeping track of the number of dosesdispensed may be the only reliable way to determine when a particularmedication canister is empty. Depression of button 46 would incrementindicator 48 to indicate the number of doses. Indicator 48 can be anysuitable indicator such as a digital display.

In another optional embodiment, inhaler system 10 may include a flowmeter 50, shown schematically in FIG. 11. Any suitable, conventionalflow meter 50 may be employed. For example, a telescoping flow meter 50can be used in conjunction with a valve between chamber 18 andmouthpiece 40 to monitor peak flow of fluid into mouthpiece 40. The flowmeter 50 can be used to ensure flow of medication to the patient, aswell as to provide the patient with an indication as to whethersufficient inhalation pressure is being exerted by the patient on themouthpiece 40 during inhalation of the medication/air mixture. This canbe an important indication since higher peak flow rates will tend toreduce deposition of medication in the mouth or oropharyngeal area ofthe patient.

Referring now to FIGS. 10-12, there are shown three views of outer part12. Outer part 12 is adapted to receive inner part 14 at least partiallywithin its structure and to form a chamber 18 in cooperation with innerpart 14 for holding a metered dose of a mixture of medication and airfor dispensing to a patient. For this purpose, outer part 12 includes amouthpiece 40 or mouthpiece attachment. In one embodiment, outer part 12includes a mouthpiece 40 as shown in FIGS. 10-12. Alternatively, aseparate mouthpiece or mask could be provided, in which case, outer part12 would be provided with a suitable mouthpiece attachment, not shown,to which the separate mouthpiece or mask could be attached. Mouthpiece40 is in fluid communication with chamber 18 for delivery of a mixtureof medication and air from chamber 18 to the mouth of a patient.Mouthpiece 40 or the mouthpiece connection can be formed as part ofeither outer part 12 or inner part 14, depending on the location on theinhaler system 10 at which the mouthpiece 40 or mouthpiece connection isto be placed, as well as the specific design of the outer and innerparts, 12, 14, respectively.

Chamber 18 may hold a volume of from about 130 to about 260 ml, morepreferably from about 140 to about 180 ml, and most preferably, about160-165 ml.

Outer part 12 also includes a recess 29 at a suitable location to allowthe user to have access to handle 30 of inner part 14, when inner part14 and outer part 12 are in the closed position of FIGS. 1-3. Recess 29can also facilitate disassembly of inhaler system 10, for cleaning, asdescribed below.

Referring to FIGS. 14-16, there are shown three views of inhaler system10 in the open position. The open position of inhaler system 10 isdesigned for insertion of a canister, as well as for use of inhalersystem 10. Thus, when a user wishes to take a dose of medication, theuser first opens cover 16, as shown in FIG. 14. The user then graspsinner part 14 by handle 30 and pulls inner part 14 in the direction ofarrows 21 until it protrudes sufficiently from outer part 12, as shownin FIG. 15, that the user can depress a canister housed in compartment20 of inner part 14. The user then places mouthpiece 40 in the user'smouth and depresses the canister to dispense a metered dose ofmedication to nozzle inlet 34. Medication is then mixed with air innozzle outlet 36, optionally as described above and the medication/airmixture passes into chamber 18 for inhalation into the lungs of the uservia mouthpiece 40. Once inhalation is completed, the user pushes innerpart 14 back into outer part 12 and closes cover 16 to provide a small,easy to carry inhaler system 10 in the closed position of FIGS. 1-3.Another advantage of the device of the present invention is that themedication canister fits completely within the device and need not beremoved from the device between doses of medication.

For cleaning, the inhaler system 10 can be easily disassembled intothree distinct parts, outer part 12, inner part 14 and cover 16, whichcan then be cleaned, for example, by soaking the parts in denturecleaning solution, with anti-bacterial soap and water, or by any othersuitable means. Cleaning of inhaler systems is important sincemedication tends to deposit on surfaces of the system and may degrade orprovide a good location for bacteria or other organisms to grow. Thus,the easy disassembly of the present device is an important advantage ofthe invention. To make cleaning easier, it is possible to fabricateinhaler system 10 from easy to clean plastic materials, such as foodgrade plastics, or other, suitable conventional materials. Also, the useof clear plastic materials to fabricate inhaler system 10 would allowthe user to see when the system requires cleaning.

An alternative embodiment of an inner part 14′ is shown in FIG. 17. Inthis embodiment, inner part 14′ includes at least two compartments 20for housing two medication canisters. Compartments 20 may be the same ordifferent. As shown in FIG. 20, two different compartments 20 areprovided, each having different widths and depths. Each compartment isequipped with a nozzle inlet 34. Alternatively, only one of theplurality of compartments 20 need be fitted with an operative nozzleinlet 34, in which case other compartments could be used for storage ofadditional canisters of medication that can be inserted into theoperative compartment 20 when dispensing of a metered dose of medicationis desired.

Suitable changes must also be made to outer part 12 to provide twonozzle inlets 36 at locations corresponding to the nozzle inlets 34 ofinner part 14′. Also, the inhaler system 10 may have to be slightlylarger for the embodiment of FIG. 17, than for other embodiments, toaccommodate the canisters' length while still providing a chamber 18having a sufficient volume for the medication/air mixture. Such changesare within the ability of an ordinarily skilled person. This embodimentallows use of two different medications with the device without havingto remove and replace a medication canister. Alternatively, twocanisters of a single medication can be carried so that when onecanister is depleted the new canister may be employed in order toprevent the patient from inadvertently running out of medication.Moreover, a separate mouthpiece specifically designed for infants can beattached to the various embodiments of the present invention if it isdesired to use the device with an infant.

The foregoing detailed description has been provided for the purpose ofillustration and description only and is not to be construed as limitingthe invention in any way. The scope of the invention is to be determinedfrom the claims appended hereto.

1. An inhaler system which comprises, an outer part, an inner partadapted to be slidably received in said outer part, said inner partcomprising a compartment of sufficient size to receive a medicationcanister and a connector for operatively connecting to said medicationcanister for dispensing of a metered dose of medication from thecanister, said inner and outer parts together forming a housing thatdefines a chamber of sufficient volume to hold a metered dose ofmedication, said chamber being in fluid communication with saidconnector, and one of said inner and outer parts including a mouthpieceor mouthpiece attachment location in fluid communication with saidchamber for permitting inhalation of medication from said chamber viasaid mouthpiece or mouthpiece attachment location.
 2. An inhaler systemas claimed in claim 1, wherein said inner part is adapted to slide asufficient distance, relative to said outer part, to permit insertion ofa canister into said compartment without disengaging said inner partfrom said outer part.
 3. An inhaler system as claimed in claim 1,wherein said connector is a universal connector.
 4. An inhaler system asclaimed in claim 1, further comprising a counter located on said housingfor providing an indication of the number of metered doses dispensedfrom a canister.
 5. An inhaler system as claimed in claim 1, furthercomprising a flow meter for providing an indication of a flow rate offluid from said chamber to said mouthpiece or mouthpiece attachmentlocation.
 6. An inhaler system as claimed in claim 1, further comprisinga cover releasably attached to said inner part.
 7. An inhaler system asclaimed in claim 6, wherein said cover includes a surface provided withinformation thereon.
 8. An inhaler system as claimed in claim 6, whereinsaid cover is pivotally attached to said inner part.
 9. An inhalersystem as claimed in claim 6, wherein said cover includes structure forcovering the mouthpiece or mouthpiece attachment location.
 10. Aninhaler system as claimed in claim 1, wherein said inhaler systemfurther comprises mixing structure located between said connector andsaid chamber.
 11. An inhaler system as claimed in claim 10, wherein saidmixing structure comprises a plurality of baffles.
 12. An inhaler systemas claimed in claim 10, wherein said mixing structure comprises aswirler.
 13. An inhaler system as claimed in claim 11, wherein saidmixing structure comprises a swirler.
 14. An inhaler system as claimedin claim 12, wherein said swirler is mounted for rotational movementabout an axis of said swirler.
 15. An inhaler system as claimed in claim1, wherein said inner part further comprises a handle to facilitatesliding said inner part relative to said outer part to move said inhalersystem from a closed position to an open position.
 16. An inhaler systemas claimed in claim 1, wherein said inner part comprises at least twocompartments for receiving canisters.